Lissencephaly with cerebellar hypoplasia (LCH): A heterogeneous group of cortical malformations

Neuropediatrics

Volumn 32, Issue 5, 2001, Pages 256-263

  Ross, M E ^a   Swanson, K ^a   Dobyns, W B ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

Author keywords

Brain malformation; Cerebellum; Genetic classification; Lissencephaly

Indexed keywords

AGYRIA; ARTICLE; BRAIN CORTEX; BRAIN MALFORMATION; CEREBELLUM HYPOPLASIA; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE CLASSIFICATION; FEMALE; GENE MUTATION; HUMAN; MALE; MOLECULAR CLONING; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPE; PRIORITY JOURNAL;

1-ALKYL-2-ACETYLGLYCEROPHOSPHOCHOLINE ESTERASE; CELL ADHESION MOLECULES, NEURONAL; CEREBELLUM; CEREBRAL CORTEX; DIAGNOSIS, DIFFERENTIAL; EXTRACELLULAR MATRIX PROTEINS; FEMALE; HIPPOCAMPUS; HUMANS; INFANT, NEWBORN; MALE; MICROCEPHALY; MICROTUBULE-ASSOCIATED PROTEINS; MUTATION; NERVE TISSUE PROTEINS; NERVOUS SYSTEM MALFORMATIONS; NEUROPEPTIDES; PHENOTYPE; SERINE ENDOPEPTIDASES;

EID: 0035213853     PISSN: 0174304X     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2001-19120     Document Type: Article

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